84257-28-3Relevant academic research and scientific papers
Synthesis of cycloalkanoindoles, the carba analogs of physostigmine
Kiraly, Imre,Hornyanszky, Gabor,Kupai, Katalin,Novak, Lajos
, p. 43 - 56 (2008/09/20)
The title compounds 9 were prepared by combined aza-Claisen rearrangement/intramolecular ring-closure reaction of N-allylaniline derivatives 3, followed by BBr3 mediated cleavage of methoxy group and subsequent formation of the phenylcarbamyl d
Enamine Chemistry. XVII. Reduction of Enaminones, Enaminothiones and Thioamides by LiAlH4 and NaBH4
Ghattas, A.-B.A.G.,Jorgensen, K. A.,Lawesson, S.-O.
, p. 505 - 512 (2007/10/02)
Enamines, 1, prepared from cycloalkanones, (cyclopentanone and cyclohexanone), and secondary amines (pyrrolidine, piperidine and morpholine), are reacted with phenylisocyanate and phenylisothiocyanate to give inseparable mixtures of enaminones (enaminothi
